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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5500379copy number variation1nstd206human GRCh38 chr11: 117,867,187-117,872,813 , GRCh37.p13 chr11: 117,737,902-117,743,528 FXYD6-FXYD2, FXYD6
    nsv5495719copy number variation1nstd206human GRCh38 chr11: 117,857,859-117,857,925 , GRCh37.p13 chr11: 117,728,574-117,728,640 FXYD6, FXYD6-FXYD2
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4989346copy number variation1nstd200human GRCh38 chr11: 117,857,085-117,947,830 , GRCh37.p13 chr11: 117,727,800-117,818,545 FXYD6, FXYD6-FXYD2, 1 more genes
    nsv4989345copy number variation1nstd200human GRCh38 chr11: 117,843,046-117,920,750 , GRCh37.p13 chr11: 117,713,761-117,791,465 FXYD6-FXYD2, TMPRSS13, 1 more genes
    nsv4847673copy number variation1nstd200human GRCh37 chr11: 117,713,761-117,791,465 , GRCh38.p12 chr11: 117,843,046-117,920,750 FXYD6, TMPRSS13, 1 more genes
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv4211035copy number variation1nstd166human GRCh37.p13 chr11: 117,729,470-117,729,524 , GRCh38.p12 chr11: 117,858,755-117,858,809 FXYD6-FXYD2, FXYD6
    nsv4209165copy number variation1nstd166human GRCh37.p13 chr11: 117,713,666-117,714,030 , GRCh38.p12 chr11: 117,842,951-117,843,315 FXYD6-FXYD2, FXYD6
    nsv3960881copy number variation1nstd168human GRCh38 chr11: 117,867,827-117,903,272 , GRCh37.p13 chr11: 117,738,542-117,773,987 FXYD6-FXYD2, TMPRSS13, 1 more genes
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3916857copy number variation2nstd102humanPathogenic NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513 RPUSD4, ELOCP22, 390 more genes
    nsv3914316copy number variation1nstd102humanPathogenic NCBI36 chr11: 115,812,352-117,422,156 , GRCh38 chr11: 116,436,425-118,046,231 , GRCh37 chr11: 116,307,142-117,916,946 LOC653303, BUD13, 31 more genes
    nsv3913230copy number variation1nstd102humanPathogenic GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630 ARHGEF12, LOC105369526, 169 more genes
    nsv3912905copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420 SLC37A2, OR6X1, 416 more genes
    nsv3911830copy number variation1nstd102humanPathogenic NCBI36 chr11: 116,182,194-134,450,377 , GRCh37 chr11: 116,676,984-134,945,165 , GRCh38 chr11: 116,806,268-135,075,271 ACRV1, BMPR1AP2, 395 more genes
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